4NVI

Predicting protein conformational response in prospective ligand discovery.

4NVI の概要

• エントリーDOI: 10.2210/pdb4nvi/pdb
• 関連するPDBエントリー: 4NVA 4NVB 4NVC 4NVD 4NVE 4NVF 4NVG 4NVH 4NVJ 4NVK 4NVL 4NVM 4NVN 4NVO
• 分子名称: Cytochrome c peroxidase, PROTOPORPHYRIN IX CONTAINING FE, 3-bromoquinolin-4-amine, ... (5 entities in total)
• 機能のキーワード: model system, flexibility, dynamic, loop, side-chains, energy penalty, occupancy, boltzmann weights, flexible docking, ligand binding, oxidoreductase
• 由来する生物種: Saccharomyces cerevisiae (Baker's yeast)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 34148.02

構造登録者

Fischer, M.,Fraser, J.S. (登録日: 2013-12-05, 公開日: 2013-12-25, 最終更新日: 2024-02-28)

主引用文献

Fischer, M.,Coleman, R.G.,Fraser, J.S.,Shoichet, B.K.
Incorporation of protein flexibility and conformational energy penalties in docking screens to improve ligand discovery.
Nat Chem, 6:575-583, 2014

PubMed Abstract: Proteins fluctuate between alternative conformations, which presents a challenge for ligand discovery because such flexibility is difficult to treat computationally owing to problems with conformational sampling and energy weighting. Here we describe a flexible docking method that samples and weights protein conformations using experimentally derived conformations as a guide. The crystallographically refined occupancies of these conformations, which are observable in an apo receptor structure, define energy penalties for docking. In a large prospective library screen, we identified new ligands that target specific receptor conformations of a cavity in cytochrome c peroxidase, and we confirm both ligand pose and associated receptor conformation predictions by crystallography. The inclusion of receptor flexibility led to ligands with new chemotypes and physical properties. By exploiting experimental measures of loop and side-chain flexibility, this method can be extended to the discovery of new ligands for hundreds of targets in the Protein Data Bank for which similar experimental information is available.

PubMed: 24950326
DOI: 10.1038/nchem.1954

実験手法

X-RAY DIFFRACTION (1.51 Å)